Genes, Neurofibromatosis 1

Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome.

Year introduced: 1992

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Subheadings:

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): G05.360.340.024.340.375.249.340, G05.360.340.024.340.415.400.340

MeSH Unique ID: D016514

Entry Terms:

• Neurofibromatosis 1 Genes
• Neurofibromatosis 1 Gene
• Genes, nf1
• Gene, nf1
• nf1 Gene
• nf1 Genes
• Genes, nf 1
• Gene, nf 1
• nf 1 Gene
• nf 1 Genes

Previous Indexing:

• Neurofibromatosis 1/genetics (1987-1991)

See Also:

• Neurofibromatosis 1
• Neurofibromin 1

All MeSH Categories
Phenomena and Processes Category
Genetic Phenomena
Genetic Structures
Genome
Genome Components
Genes
Genes, Neoplasm
Genes, Tumor Suppressor
Genes, Neurofibromatosis 1

All MeSH Categories
Phenomena and Processes Category
Genetic Phenomena
Genetic Structures
Genome
Genome Components
Genes
Genes, Recessive
Genes, Tumor Suppressor
Genes, Neurofibromatosis 1